- PII
- S3034630425070061-1
- DOI
- 10.7868/S3034630425070061
- Publication type
- Article
- Status
- Published
- Authors
- Volume/ Edition
- Volume 61 / Issue number 7
- Pages
- 848-856
- Abstract
- A convenient synthetic approach has been developed for novel monobenzotriazoles incorporating a mesoionic 1,3a,6,6a-tetraazapentalene core. The method involves a Cu(I)-catalyzed (3+2) cycloaddition of ortho-nitrophenyl azide to terminal aryl(alkyl)acetylenes, followed by an intramolecular cyclization under Cadogan-type deoxygenation conditions. The process can be successfully performed in a one-pot fashion, affording the target benzo[d][1,2,3]triazolo[1,2-a]triazole derivatives in good yields.
- Keywords
- клик-реакция дезоксигенирование реакция Кадогана тетраазапенталены
- Date of publication
- 01.07.2025
- Year of publication
- 2025
- Number of purchasers
- 0
- Views
- 23
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